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RECALL RECORD — CLASS IRecall closedF-1230-2013/FDA enforcement
Dymatize Enterprises, LLC·Food·May 3, 2012

Dymatize Nutrition Xpand Post Xtreme Mass Recovery System Fruit Punch 3.5 lb Manufactured &…

What you need to know

Class I

  • What happened

    The product label declares whey but does not declare milk.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDAINMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameDymatize Enterprises, LLC
Recalling firmDymatize Enterprises, LLCFarmers Branch, TX, United States
UPC / barcodes
7 05016 89562 5
Lot / date codes
  • Lots 1244003, 1292006, 1340011, 1021107, 1075104, 1151111, and 1307105.
Distribution area
IN

Product was distributed in the United States, Algeria, Australia, Bulgaria, Canada, Cyprus, Czech Republic, Dominican Republic, France, French Polynesia, Germany, Indonesia, Italy, Jordan, Korea, Mexico, Netherlands, Philipines, Portugal, Puerto Rico, Qatar, Russia, Slovenija, South Africa, Spain, Sweden, Switzerland, Thailand, Turkey, and United Kingdom.

United States, Canada, Mexico, United Kingdom, Australia, Germany, France, Puerto Rico

Quantity affected13, 768 units
Recall initiationFDA report date: March 27, 2013
FDA recall numberF-1230-2013

Beyond the headline

The recall, in context

Dymatize Enterprises, LLC initiated this food recall on May 3, 2012. The FDA enforcement report states: The product label declares whey but does not declare milk. The FDA report lists distribution as: Product was distributed in the United States, Algeria, Australia, Bulgaria, Canada, Cyprus, Czech Republic, Dominican Republic, France, French Polynesia, Germany, Indonesia, Italy, Jordan, Korea, Mexico, Netherlands, Philipines, Portugal, Puerto Rico, Qatar, Russia, Slovenija, South Africa, Spain, Sweden, Switzerland, Thailand, Turkey, and United Kingdom.

The FDA enforcement report describes the reason as: The product label declares whey but does not declare milk.

Dymatize Nutrition Xpand Post Xtreme Mass Recovery System Fruit Punch 3.5 lb Manufactured &… was made or distributed by Dymatize Enterprises, LLC in Farmers Branch, TX, United States. This page reflects FDA report F-1230-2013, dated March 27, 2013.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared milk

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a milk allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed cow's milk allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a milk allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Dymatize Nutrition Xpand Post Xtreme Mass Recovery System Fruit Punch 3.5 lb Manufactured &… recall?

Dymatize Enterprises, LLC recalled Dymatize Nutrition Xpand Post Xtreme Mass Recovery System Fruit Punch 3.5 lb Manufactured &… in an FDA Class I enforcement action reported as F-1230-2013. The product label declares whey but does not declare milk.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Do not eat the product if you have a milk allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Dymatize Enterprises, LLC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1230-2013. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Dymatize Enterprises, LLC

View brand
Class I·

Dymatize Enterprises, LLC

Dymatize Nutrition Xpand Post Xtreme Mass Recovery System Lemonade 3.5 lb Manufactured &…

The product label declares whey but does not declare milk.

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Class I·

Dymatize Enterprises, LLC

Dymatize Nutrition Xpand Post Xtreme Mass Recovery System Blue Raspberry 3.5 lb Manufactured &…

The product label declares whey but does not declare milk.

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.